Detailed information for compound 377139

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 1362.64 | Formula: C64H99N17O14S
  • H donors: 14 H acceptors: 13 LogP: -1.34 Rotable bonds: 53
    Rule of 5 violations (Lipinski): 4
  • SMILES: NCCCC[C@H](C(=O)N1CCC[C@@H]1C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@H](C(=O)OC)CCSC)CC(C)C)Cc1ccccc1)Cc1ccccc1)CCC(=O)N)CCC(=O)N)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)N
  • InChi: 1S/C64H99N17O14S/c1-38(2)34-46(57(88)77-45(28-33-96-4)63(94)95-3)73-53(84)37-72-54(85)47(35-39-16-7-5-8-17-39)78-58(89)48(36-40-18-9-6-10-19-40)79-56(87)42(24-26-51(67)82)74-55(86)43(25-27-52(68)83)75-59(90)50-23-15-32-81(50)62(93)44(21-11-12-29-65)76-60(91)49-22-14-31-80(49)61(92)41(66)20-13-30-71-64(69)70/h5-10,16-19,38,41-50H,11-15,20-37,65-66H2,1-4H3,(H2,67,82)(H2,68,83)(H,72,85)(H,73,84)(H,74,86)(H,75,90)(H,76,91)(H,77,88)(H,78,89)(H,79,87)(H4,69,70,71)/t41-,42-,43-,44-,45-,46-,47-,48-,49-,50?/m0/s1
  • InChiKey: CWWARWOPSKGELM-VSBOMFCXSA-N  


Substructure search Similarity search

Network

Hover on a compound node to display the structore

Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

No curated genes were found associated with this compound

Predicted pathogen targets for this compound

By orthology
No druggable targets predicted by orthology data
By sequence similarity to non orthologous known druggable targets
No druggable targets predicted by sequence similarity
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Plasmodium vivax telomerase reverse transcriptase, putative 0.0867 0.2571 1
Giardia lamblia Telomerase catalytic subunit 0.0867 0.2571 0.5
Trypanosoma brucei telomerase reverse transcriptase 0.0867 0.2571 1
Toxoplasma gondii RNA-directed DNA polymerase 0.0867 0.2571 1
Mycobacterium ulcerans hydrolase 0.0068 0 0.5
Schistosoma mansoni tyrosine kinase 0.008 0.0036 0.002
Echinococcus multilocularis arachidonate 5 lipoxygenase 0.0137 0.0219 0.1392
Schistosoma mansoni hypothetical protein 0.008 0.0036 0.0025
Toxoplasma gondii 3'5'-cyclic nucleotide phosphodiesterase domain-containing protein 0.0489 0.1356 0.5018
Brugia malayi Hemopexin family protein 0.008 0.0036 0.005
Echinococcus granulosus matrix metallopeptidase 7 M10 family 0.0204 0.0438 0.3049
Schistosoma mansoni high-affinity cgmp-specific 35-cyclic phosphodiesterase 0.0489 0.1356 1
Loa Loa (eye worm) matrixin family protein 0.0136 0.0217 0.4095
Echinococcus multilocularis calcium:calmodulin dependent 3',5' cyclic 0.0233 0.0531 0.3752
Loa Loa (eye worm) TK/EGFR protein kinase 0.0148 0.0256 0.4826
Echinococcus granulosus arachidonate 5 lipoxygenase 0.0137 0.0219 0.1392
Echinococcus multilocularis calcium:calmodulin dependent 3',5' cyclic 0.0109 0.0132 0.073
Onchocerca volvulus Matrilysin homolog 0.0125 0.0181 0.0145
Brugia malayi Telomerase reverse transcriptase 0.2306 0.7208 1
Echinococcus multilocularis high affinity cgmp specific 3' 5' cyclic 0.0489 0.1356 1
Echinococcus multilocularis epidermal growth factor receptor 0.0148 0.0256 0.1671
Trypanosoma cruzi telomerase reverse transcriptase, putative 0.0867 0.2571 1
Brugia malayi Furin-like cysteine rich region family protein 0.0148 0.0256 0.0355
Plasmodium falciparum telomerase reverse transcriptase 0.0867 0.2571 1
Brugia malayi Matrixin family protein 0.0136 0.0217 0.0302
Echinococcus granulosus calcium:calmodulin dependent 3'5' cyclic 0.0109 0.0132 0.073
Schistosoma mansoni lipoxygenase 0.0095 0.0087 0.0409
Loa Loa (eye worm) matrixin family protein 0.0125 0.0181 0.3413
Brugia malayi Probable 3',5'-cyclic phosphodiesterase T04D3.3, putative 0.0233 0.0531 0.0736
Onchocerca volvulus Matrix metalloproteinase homolog 0.0125 0.0181 0.0145
Leishmania major telomerase reverse transcriptase, putative 0.0867 0.2571 1
Schistosoma mansoni lipoxygenase 0.0137 0.0219 0.1409
Schistosoma mansoni tyrosine kinase 0.008 0.0036 0.002
Schistosoma mansoni matrix metallopeptidase-9 (M10 family) 0.0082 0.0044 0.0085
Trypanosoma cruzi telomerase reverse transcriptase, putative 0.0867 0.2571 1
Echinococcus granulosus high affinity cgmp specific 3' 5' cyclic 0.0489 0.1356 1
Echinococcus granulosus epidermal growth factor receptor 0.0148 0.0256 0.1671
Mycobacterium leprae PROBABLE HYDROLASE 0.0068 0 0.5
Loa Loa (eye worm) PDE1B protein 0.0233 0.0531 1
Mycobacterium tuberculosis Probable peptidoglycan hydrolase 0.0068 0 0.5
Schistosoma mansoni calcium/calmodulin-dependent 35-cyclic nucleotide phosphodiesterase 0.0233 0.0531 0.3765
Schistosoma mansoni tyrosine kinase 0.0148 0.0256 0.1688
Echinococcus granulosus calcium:calmodulin dependent 3'5' cyclic 0.0233 0.0531 0.3752
Echinococcus multilocularis matrix metallopeptidase 7 (M10 family) 0.0204 0.0438 0.3049

Activities

Activity type Activity value Assay description Source Reference
Alphax10E (functional) = 1 Intrinsic activity was measured on the dog carotid artery. ChEMBL. 6177855
Alphax10E (functional) = 1 Intrinsic activity was measured on the rabbit mesenteric vein. ChEMBL. 6177855
Alphax10E (functional) = 1 Intrinsic activity was measured on the guinea pig ileum. ChEMBL. 6177855
pD2 (functional) = 6.95 Apparent affinity was measured on the rabbit mesenteric vein. ChEMBL. 6177855
pD2 (functional) = 8.47 Apparent affinity was measured on the guinea pig ileum. ChEMBL. 6177855
pD2 (functional) = 9.19 Apparent affinity was measured on the dog carotid artery. ChEMBL. 6177855
RA (functional) = 15.5 Relative affinity compared to substance P was measured in the dog carotid artery. ChEMBL. 6177855
RA (functional) = 25.1 Relative affinity compared to substance P was measured in rabbit mesenteric vein. ChEMBL. 6177855
RA (functional) = 49 Relative affinity compared to substance P was measured in guinea pig ileum. ChEMBL. 6177855
RP (functional) = 69 Relative potency compared substance P - change in blood pressure in anesthetized rat. ChEMBL. 6177855
SP (functional) = 13.6 % Evaluated in vitro for percent agonist activity in guinea pig ileum (substance P receptor) ChEMBL. 2433442
SP (functional) = 16 % Evaluated in vitro for percent agonist activity in guinea pig ileum (substance P receptor) ChEMBL. 2433442

Phenotypes

Whole-cell/tissue/organism interactions

We have no records of whole-cell/tissue assays done with this compound What does this mean?

Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.

Annotated phenotypes:

We have no manually annotated phenotypes for this drug. What does this mean? / Care to help?
In TDR Targets, information about phenotypes that are caused by drugs, or by genetic manipulation of cells (e.g. gene knockouts or knockdowns) is manually curated from the literature. These descriptions help to describe the potential of the target for drug development. If no information is available for this gene or if the information is incomplete, this may mean that i) the papers containing this information either appeared after the curation effort for this organism was carried out or they were inadvertently missed by curators; or that ii) the curation effort for this organism has not yet started.
 
In any case, if you have information about papers containing relevant validation data for this target, please log in using your TDR Targets username and password and send them to us using the corresponding form in this page (only visible to registered users) or contact us.

External resources for this compound

Bibliographic References

2 literature references were collected for this gene.

If you have references for this compound, please enter them in a user comment (below) or Contact us.